reference/35245472

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/35245472

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endingPage	27
issn	1381-6810 1744-5094
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publicationName	Ophthalmic Genetics
startingPage	19
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bibliographicCitation	Wang D, Trevillian P, May S, Diakumis P, Wang Y, Colville D, Bahlo M, Greferath U, Fletcher E, Young B, Mack HG, Savige J. KCTD1 and Scalp-Ear-Nipple ('Finlay-Marks') syndrome may be associated with myopia and Thin basement membrane nephropathy through an effect on the collagen IV α3 and α4 chains. Ophthalmic Genet. 2023 Feb;44(1):19–27. doi: 10.1080/13816810.2022.2144900. PMID: 36579937.
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date	2022-12-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://doi.org/10.1080/13816810.2022.2144900 https://pubmed.ncbi.nlm.nih.gov/36579937
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language	English
source	https://pubmed.ncbi.nlm.nih.gov/ https://www.crossref.org/
title	KCTD1 and Scalp-Ear-Nipple (‘Finlay–Marks’) syndrome may be associated with myopia and Thin basement membrane nephropathy through an effect on the collagen IV α3 and α4 chains
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